SERYNTH FUNGI NAIL by Jiangxi Hemei Pharmaceutical Co., Ltd 84010-232complete

SERYNTH FUNGI NAIL by

Drug Labeling and Warnings

SERYNTH FUNGI NAIL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SERYNTH FUNGI NAIL- tolnaftate 1% fungi nail liquid 
Jiangxi Hemei Pharmaceutical Co., Ltd

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84010-232complete

Active Ingredient

Tolnaftate 1%

Purpose

Antifungal

Use

Soothes most Athlete's Foot (Tinea Pedis)
and Ringworm (Tinea Corporis). Relieves
itching, scaling, cracking, burning,
redness, sorenes, and irritation
discomfort. Helps prevent most athlete's
foot (dermatophytosis) with daily use.

Warnings

For external use only.

Do not use

on children under 2 years of age unless directed by a doctor.

When Using

avoid contact with eyes.

Stop Use

irritation occurs, there is no improvement within 4 weeks (for athlete's foot and ringworm).

Ask Doctor

irritation occurs, there is no improvement within 4 weeks (for athlete's foot and ringworm).

Keep Oot Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For athlete's foot and ringworm
: use daily for 4 weeks. Clean the
affected area and dry thoroughly. Apply
a thin layer of the product over affected
area twice daily (morning and night) or as directed by a doctor. Supervise children
in the use of this product. This product
is not effective for the precention of ringworm
of the scalp or nails. For athlete's
foot: pay special attention to spaces
between the toes, wear well-fitting, ventilated
shoes, and change shoes and
socks at least once daily. To prevent
athlete's foot, apply once or twice daily
(morning and/or night). Apply to skin
around the nail and cuticle.

Other information

Store at room temperature 15°-30℃ (59-86℉)

Inactive ingredients

Water, Euphorbia Hirta whole, Glycerin, Hydracrylic Acid, Pseudolarix Amabilis bark, Resorcinol.

SERYNTH FUNGI NAIL 
tolnaftate 1% fungi nail liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-232
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EUPHORBIA HIRTA WHOLE (UNII: L13YF113GN)
RESORCINOL (UNII: YUL4LO94HK)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRACRYLIC ACID (UNII: C4ZF6XLD2X)
PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-232-01	15 mL in 1 TUBE; Type 0: Not a Combination Product	12/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	12/09/2025	02/08/2026

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-232)

Revised: 2/2026

Document Id: 4a4629a9-4bbf-4b1b-e063-6394a90a46db

34390-5

Set id: 457d2aae-eed2-4ed3-e063-6394a90adb2b

Version: 2

Effective Time: 20260207